Substituted benzyl-thiolcarbamic acid esters

ABSTRACT

Substituted benzyl-thiolcarbamic acid esters, i.e., S-((alkoxy)(optionally chloro, bromo, nitro and alkyl substituted)-benzyl)(N-alkyl and N,N-dialkyl)-thiolcarbamic acid esters and S((alkoxy)-(optionally chloro, bromo, nitro and alkyl substituted)-benzyl)-(pyrrolidino and piperidino)-carbothiolic acid esters, which possess herbicidal properties and which may be produced by conventional methods.

United States Patent [1 1 Kudamatsu et al.

114 *Nov. 4, 1975 SUBSTITUTED BENZYL-THIOLCARBAMIC ACID ESTERS [75] Inventors: Akio Kudamatsu; Masao Miyamoto;

Nobuo Fukazawa, all of Tokyo, Japan [73] Assignee: Bayer Aktiengesellschaft,

Leverkusen, Germany Notice: The portion of the term of this patent subsequent to Dec. 3, 1991, has been disclaimed.

[22] Filed: Feb. 21, 1974 [21] Appl. No.: 444,603

Related US. Application Data [60] Division of Ser. No. 170,655, Aug. 10, 1971, Pat. No. 3,852,318, which is a continuation of Ser. No. 875,546, Nov. 10, 1969, abandoned.

[30] Foreign Application Priority Data Nov. 12, 1968 Japan 43-82249 [52] US. Cl. 260/293.73 [51] Int. Cl. C07D 295/16 [58] Field of Search EEO/293.73, 326.4, 455 A [56] References: Cited UNITED STATES PATENTS 3,133,947 5/1964 Tilles 260/455 A FOREIGN PATENTS OR APPLICATIONS 201,380 11/1967 U.S.S.R 260/455 A Primary Examiner-Sherman D. Winters Attorney, Agent, or FirmBurgess, Dinklage & Sprung 57 ABSTRACT 3 Claims, No Drawings SUBSTITUTED BENZYL-THIOLCARBAMIC ACID ESTERS This is a division, of application Ser. No. 170,655, filed Aug. 10, 1971, now US. Pat. No. 3,852,318 which is a streamlined continuation of application Ser. No. 875,546, filed Nov. 10, 1969, now abandoned.

The present invention relates to and has for its objects the provision for particular new substituted benzylthiolcarbamic acid esters, i.e., S-[(alkoxy)-(optionally chloro, bromo, nitro andalkyl substituted)-benzyl]-[N-alkyl and N,N-dialkyl]-thiolcarbamic acid esters and S-[(alkoxy)-(optionally chloro, bromo, nitro and alkyl substituted)-benzyl]-[pyrrolidino and piperidino]-carbothiolic acid esters, which possess herbicidal properties, active compositions in the form of mixtures of such compounds with solid and liquid dispersible carrier vehicles, and methods for producing such compounds and for using such compounds in a new way, especially for combating weeds, e.g. undesired plants and the like, with other and further objects becoming apparent from a study of the within specification and accompanying examples.

It is already known that pentachloro-phenol (A), which may be designated PCP, and 2-methyl-4-chlorophenoxyacetic acid (B), which may be designated MCP, as well as S-benzyl-N,N-dimethyl-dithiocarbamate (C), which may be designated T, possess herbicidal properties.

Pentachlorophenol (A), i.e., PCP, is used for controlling barnyard grass. However, PCP possesses disadvantages such as an irritant effect on human skin and mucous membranes and specific toxicity to fish and shells, which limit the application periods and fields of use of such compound. To control spikerushes (Eleocharis acicularis) which commonly grow together with bamyard grass (Echinochloa crus-galli), 2-methyl-4-chlorophenoxyacetic acid (B), i.e., MCP, is used, but this compound is not effective in controlling barnyard grass.

Accordingly, in order to control simultaneously both barnyard grass and spikerushes, the main types of weeds found in paddy fields, a mixture of PCP and MCP is generally used.

It is furthermore known from French Pat. No. 1,328,1 12 that benzyl dialkylthiocarbamates, i.e benzyl, di-butyl, di-iso-propyl-, di-n-propyl and di-ethylthiocarbamate possess herbicidal properties. In said French Patent it is indicated that benzyl di-iso-propyl thiocarbamate (D) is an active herbicide against wild oats (Avena fatua).

It has now been found, in accordance with the present invention, that the particular new substituted benzyl-thiolcarbamic acid esters of the formula R is alkyl of l-'4 carbon atoms,

X is hydrogen, chloro, bromo, nitro or alkyl of 1-4 carbon atoms, and

Y is alkylamino'having l-4 carbon atoms, dialkylamino having l-4 carbon atoms in each alkyl moiety, pyrrolidino or piperidino,

in which a R and X are the same as defined above, and M is a hydrogen or an alkali metal such as sodium or potassium, and the like, especially sodium, with a carbamyl chloride of the formula Cl Y (III) in which Y is the same as defined above;

or a reacting an alkoxy-benzyl mercaptan of the formula CH2SH X in which R and X are the same as defined above, with an isocyanate of the formula OCN-Y' (III') in which Y is alkyl of l4 carbon atoms;

or b. reacting an alkoxy-benzyl halide of the formula in which I Rand X are the same as defined above, and Hal is a halogen atom such as chloro, bromo, iodo or fluoro, especially chloro, with carbonylsulfide of the formula 1 COS and with an amine of the formula in which Y is the same as defined above, in the presence of a base of the formula v 3 in which i v M is alkali metal such as sodium, potassium, and the like," especially sodium; or c. reacting an-alkoxy-be'nzyl thiolcarbonyl chloride of the formula I ll CH S-CCl X in which (VIII) (VIII) weeds in paddy rice fields, particularly barnyard grass and spikerushes, and exhibit a remarkable effect in killing such weeds, with only slight, if any, phytotoxic effect toward cultivated plants suchas rice. The instant compounds also show acaricidal and nematocidal effectiveness. The instant compounds therefore represent a valuable contribution to the art.

Advantageously, in accordance with the present invention, in the various formulae herein:

R represents straight and branched chain lower alkyl hydrocarbon of 1-4 carbon atoms such as methyl, ethyl, nand iso-propyl, n-, iso-, sec.- and ten.- butyl, and the like, especially C or C alkyl; X represents hydrogen, chloro, i.e., mand pchloro, especially 3- and chloro,

bromo, i.e., o-, mand pbromo, especially S-bromo,

nitro, i.e., o-, mand pnitro, especially 3-nitro, or straight and branched chain lower alkyl hydrocarbon of 1-4 carbon atoms such as methyl to tert.-butyl inclusive, as defined above, and the like, i.e., o-, mand p- C alkyl, especially C or C alkyl, and more espe cially 3-and 5- C alkyl; and

Y represents alkylamino having l'4 carbon atoms such as methyl to tert.-butyl inclusive, as defined above, -amino, and the like, especially C or C alkylamino,

dialkylamino having 1-4 carbon atoms in each alkyl radical such as di (same and mixed) methyl to tert.- butyl inclusive, as defined above, -amino, and the like, especially di (same and mixed) C or C alkyl amino,

pyrrolidino, or

piperidino.

Preferably, R is C alkyl; X is hydrogen; or chloro; or bromo;' or nitro; or C alkyl; and Y is C alkylamino; or di C alkylamino; or pyrrolidino; or piperidino. 1,

In particular, Ris C alkyl; X is hydrogen; or chloro; or bromo; .or C alkyl; and Y is C alkylamino; or di C alkylamino;,or pyrrolidino; or piperidino.

The reaction courses according to process variants (a), (b) and (c) are illustrated by the following respective formula schemes: 1

(III) CH -Hal COS H-Y M OH (V) (VI) (VII) The starting materials which may be used for reaction variants (a), (b) and (c) are clearly characterized by formulae (II), (III), (IV), (V), (VI), (VII) and (VIII) above, and are well known.

As examples of alkoxy-benzyl mercaptans and mercaptides of formula (II) above which may be used as starting materials, there are mentioned: 2-, 3- and 4- methoxy, ethoxy, nand iso-propoxy,- n, iso-, sec.- and tert.-butoxy-(optionally 3- or'5- chloro, bromo, nitro, methyl, ethyl, nand iso-propyl, n-, iso-, sec.- and tert.- butyl)-benzyl mercaptans and the corresponding sodium mercaptides, and the like.

chloro, bromo, nitro, methyl, ethyl, nand iso-propyl,

n-, iso-', sec.- and tert.-butyl)-benzyl chlorides, bromides, iodides and fluorides, and the like.

As examples of amines of formula (VI) above which may be used as starting materials, there are mentioned: mono and di (same and mixed) methyl, ethyl, nand iso-propyl, n-, iso-, sec.- and tert.-butyl amines, pyrrolidine and piperidine, and the like.

As examples of bases of formula VII above which may be used as starting materials, there may be mentioned: sodium, potassium, etc., hydroxides, and the like.

As examples of alkoxy-benzyl thiolcarbonyl chlorides of formula (VIII) above which may be used as starting materials, there are mentioned: 2-, 3- and 4-methoxy, ethoxy, nand iso-propoxy, n-, iso-, sec.- and tert.- butoxy-(optionally 3- or 5-chloro, bromo, nitro, methyl, ethyl, nand iso-propyl, n-, iso, sec.- and tert.- butyl)-benzyl thiolcarbonyl chlorides, and the like.

The process according to each of the variants is preferably carried out in the presence of an inert organic solvent (this term includes a mere diluent). Examples of such solvents include aliphatic or aromatic hydrocarbons (which may be halogenated), for example benzine, methylene chloride, chloroform, carbon tetrachloride, benzene, chlorobenzene, toluene, and xylene; ethers, for example diethyl ether, dibutyl ether, dioxan, and tetrahydrofuran; aliphatic alcohols or ketones which have low boiling points, for example methanol, ethanol, isopropanol, acetone, methyl ethyl ketone, methyl isopropyl ketone, and methyl isobutyl ketone; and the like. Lower aliphatic nitriles, for example acetonitrile, propionitrile, and the like, may also be used.

If M is hydrogen in the appropriate starting compound of formula (II) above, the reaction according to variant (a) may preferably be carried out in the presence of an acid-binding agent. Examples of these include alkali metal carbonates and bicarbonates or alcoholates, such as potassium carbonate, sodium bicarbonate, sodium carbonate, or sodium or potassium methylate or ethylate, or aliphatic, aromatic or heterocyclic tertiary bases such as triethylamine, diethylaniline, pyridine, and the like.

The reaction according to all of the process variants may be carried out within a fairly wide temperature range, but in general at temperatures from substantially between about OlO0C, preferably between about 60C.

are not desired. Whether the active compounds according to the present invention act as total or selective herbicidal agents depends on the amount applied, as the artisan will appreciate.

The active compounds according to the present invention can be used for example in the case of the following plants: dicotyledons, such as mustard (Sinapis), cress (Lepidium), catch weed (Galium), common chickweed (Stellaria), camomile (Matricaria), French weed (Galinsoga), goose-foot (Chenopodium), stinging nettle (Urtica), groundsel (Senecio), wild amaranth (Amaranthus), common purslane (Portulaca), cotton (Gossyppium), beets (Beta), carrots (Daucus), beans (Phaseolus), potatoes (Solarium), coffee (Coffea), cabbage (Brassica), spinach (Spinacia); monocotyledons, such as timothyl (Phleum), meadowgrass (Poa), fescue (Festuca), finger grass (Digitaria), goosegrass (Eleusine), green foxtail (Setaria), raygrass (lolium),

cheat (Bromis), barnyard grass (Echinochloa), maize (Zea), rice (Oryza), oats (Avena), barley (I-Iordeum), wheat (Triticum), millet (Panicum) and sugar cane (Saccharum); and the like.

In particular, broad le aved weeds such as Monochoria vaginalis, Rotala indica, Lindernia pyxidaria, Gratiola japonica, and the like, may be controlled by the active In carrying out process variant (a) one may for examally colorless or light yellow chemical substances which are hardly soluble in water, yet soluble in organic solvents, such as alcohol, ketone, benzene, etc.

Advantageously, the instant active compounds exhibit a strong herbicidal potency and can therefore be used as weed-killers. By weeds in the sense used herein are meant all plants which grow in places where they compounds of the present invention.

The instant compounds are preferably used as selective herbicides and especially when applied to soil before germination, although they exhibit a particularly good selectivity when applied either before or after emergence.

The instant active compounds possess excellent herbicidal properties, being especially effective in the control of weeds in paddy fields, particularly barnyard grass and spikerushes. Thus, when barnyard grass is treated in its pre-emergence stage or in its one to three leaf stage under irrigated conditions with the present compounds, such compounds are found to exhibit a strong herbicidal effect. This is technically of great importance, because most of the herbicides now on the market are only effective against barnyard grass before or immediately after germination. Moreover, since the instant compounds are less phytotoxic to rice plants, they can be applied 1 to 2 weeks after the transplantation of rice plants to control weeds in paddy fields, for which time span no appropriate weed-controlling method has been found heretofore, the latter being a great advantage in connection with labor-saving considerations in agricultural cultivation.

Since the compounds of the present invention possess, in particular, strong herbicidal activity by reason of root-absorption, they can also be utilized effectively as non-selective or selective herbicides (depending on their application methods) against weeds growing in places other than paddy fields.

Furthermore, the present compounds are effective acaricides, eg when applied to plants, especially against spider mites, including resistant strains, substantially without phytotoxicity to the plants.

It is also possible to control rice white-tip nematodes with the instant active compounds, e.g. by treating seed contaminated therewith.

The active compounds according to the instant invention can be utilized, if desired, in the form of the usual formulations or compositions with conventional inert (i.e., plant compatible or herbicidally inert) pesticide diluents or extenders, i.e., diluents or extenders of the type usable in conventional pesticide formulations or compositions, e.g. conventional pesticide dispersible carrier vehicles, such as solutions, emulsions, suspensions, emulsifiable concentrates, spray powders, pastes, soluble powders, dusting agents, granules, etc. These are prepared in known manner, for instance by extending the active compounds with conventional pesticide dispersible liquid diluent carriers and/or dispersible solid carriers optionally with the use of carrier vehicle assistants, e.g. conventional pesticide surface-active agents, including emulsifying agents and/or dispersing agents, whereby, for example, in the case where water is used as diluent, organic solvents may be added as auxiliary solvents. The following may be chiefly considered for use as conventional carrier vehicles for this purpose: inert dispersible liquid diluent carriers including inert organic solvents, such as aromatic hydrocarbons (e.g. benzene, toluene, xylene, etc.), halogenated, especially chlorinated, aromatic hydrocarbons (e.g. chlorobenzenes), paraffins (e.g. petroleum fractions), chlorinated aliphatic hydrocarbons (e.g. methylene chloride, etc.), alcohols (e.g. methanol, ethanol, propanol, butanol, etc.), ethers, ether-alcohols (e.g. glycol monomethyl ether, etc.), amines (e.g. ethanol-amine, etc.), amides (e.g. dimethyl formamide, etc.), sulfoxides (e.g. dimethyl sulfoxide, etc.), ketones (e.g. acetone, etc.), and/or water; as well as inert dispersible finely divided solid carriers, such as ground natural minerals (e.g. kaolins, alumina, silica, chalk, i.e., calcium carbonate, talc, kieselguhr, montmorillonite, clay, etc.), and ground synthetic minerals (e.g. highly dispersed silicic acid, silicates, e.g. alkali silicates, etc. whereas the following may be chiefly considered for use as conventional carrier vehicle assistants, e.g. surface-active agents, for this purpose: emulsifying agents, such as non-ionic and/or anionic emulsifying agents (e. g. polyethylene oxide esters of fatty acids, polyethylene oxide ethers of fatty alcohols, alkyl sulfonates, aryl sulfonates, etc., and especially alkyl aryl-polyglycol ethers, magnesium stearate, sodium oleate, etc.); and- /or dispersing agents, such as pulp sulfite waste liquors, methyl cellulose, lignin, etc.

As will be appreciated by the artisan, the active compounds according to the instant invention may be em- .ployed alone or in the form of mixtures with one another and/or with such solid and/or liquid dispersible carrier vehicles and/or with other known compatible active agents, especially plant protection agents, such as other herbicides, insecticides, acaricides and nematocides, or fungicides, bactericides, plant growth regulators, soil disinfectants, including phenoxy compounds, chlorophenol compounds, carbamates, diphenyl ethers, urea compounds, triazine compounds, and other known agricultural chemicals and/or fertilizers, etc., if desired, or in the form of particular dosage preparations for specific application made therefrom, such as solutions, emulsions, suspensions, powders, pastes, and granules which are thus ready for use.

As concerns commercially marketed preparations, these generally contemplate carrier composition mixtures in which the active compound is present in an amount substantially between about 0.1 and 95 percent by weight, and preferably 0.5 and 90 percent by weight, of the mixture, whereas carrier composition mixtures suitable for direct application or field application generally contemplate those in which the active compound is present in an amount substantially between about 0.001-30 percent, preferably 0.05-10 percent, by weight of the mixture. Thus, the present invention contemplates over-all compositions which comprise mixtures of a conventional dispersible carrier vehicle such as (1) a dispersible inert finely divided carrier solid, and/or (2) a dispersible carrier liquid such as an inert organic solvent and/or water preferably including a surface-active effective amount of a carrier vehicle assistant, e.g. a surface-active agent, such as an emulsifying agent and/or a dispersing agent, and an amount of the active compound which is effective for the purpose in question and which is generally between about 0.001- percent, and preferably 0.05-95 percent, by weight of the mixture.

In particular, the amount of active compound applied per unit area varies according to the purpose intended, i.e., the effect desired, and the mode of application. In general, higher quantities of substantially between about 640 kg of active compound per hectare are applied for total or non-selective herbicidal activity, whereas lower quantities of substantially between about 1.25-5 kg of active compound per hectare are applied for selective herbicidal activity, i.e., irrespective of the presence or absence of the carrier vehicle.

The active compounds can also be used in accordance with the well-known ultra-low-volume process with good success, i.e., by applying such compound if normally a liquid, or by applying a liquid composition containing the same, via very effective atomizing equipment, in finely divided form, e.g. average particle diameter of from 50-100 microns, or even less, i.e., mist form, for example by airplane crop spraying techniques. Only up to at most about a few liters/hectare are needed, and often amounts only up to about 1 quatlacre, preferably 2-16 fluid ounces/acre, are sufficient. In this process it is possible to use highly concentrated liquid compositions with said liquid carrier vehicles containing from about 20 to about 95 percent by weight of the active compound or even the percent active substance alone, e.g. about 20400 percent by weight of the active compound.

While the active compounds can be used as herbicides particularly effectively according to the preemergence method, they are also effective when used according to the post-emergence method.

Especially when application is carried out mainly before the germination of cultivated plants, the general conditions of cultivation are not so important, but the quantity of active compound to be applied per unit area and the application method are important, as the artisan will appreciate.

Furthermore, the present invention contemplates methods of selectively killing, combatting or controlling undesired plants, e.g. weeds, and the like, which comprise applying to at least one of (a) such weeds and (b) their habitat, i.e., the locus to be protected, a herbicidally effective or toxic amount of the particular active compound of the invention alone or together with a carrier vehicle as noted above. The instant formulations or compositions are applied in the usual manner, for example by spraying, atomizing, scattering, dusting, watering, sprinkling, pouring, dressing, and the like.

It will be realized, of course, that the concentration of the particular active compound utilized in admixture with the carrier vehicle will depend upon the intended application and may be varied within a fairly wide range depending upon the weather conditions, the soil, the purpose for which the active compound is used, e.g. for total or only selective herbicidal effect, and the plants which are to be controlled or protected. Therefore, in special cases, it is possible to go above or below the aforementioned concentration ranges and amounts per unit area.

The following illustrate, without limitation, examples of formulations which may be used in accordance with the present invention:

FORMULATION A percent by weight of instant compound (1), and 95 percent by weight of a mixture of talc and clay (3:1) are formulated into a dust by mixing and crushing. It is applied as is by dusting to weeds and/or their habitat.

FORMULATION B percent by weight of instant compound (17), 75 percent by weight of talc and clay (3:2), 3 percent by weight of sodium alkylbenzene sulfonate, and 2 percent by weight of sodium dinaphthylmethane disulfonic acid, are formulated into a wettable powder by mixing and crushing. It is diluted with water at the concentration of l to 500, and applied by spraying to weeds and- /or their habitat.

FORMULATION C 20 percent by weight of instant compound (18), 75 percent by weight of xylol, and 5 percent by weight of emulsifier Sorpol (trade name of the product of Toho Kagaku Kogyo I(.K., Japan; polyoxyethylenealkylarylether) are formulated into an emulsifiable concentrate by mixing and stirring. It is diluted with water at the concentration of l to 1,000, and applied by spraying to weeds and/or their habitat.

FORMULATION D EXAMPLE. 1

Test against weeds of paddy fields Preparation of active compounds:

Carrier vehicle 5 parts by weight of acetone 5 parts by weight of talc 1 part by weight of benzyloxypolyglycolether To produce a suitable preparation of the particular active compound, 1 part by weight of such active compound is mixed with the stated amount of carrier vehicle and the stated amount of emulsifier intimately, and the resulting emulsifiable concentrate or wettable powder is then diluted with water to the desired final concentration.

Test method:

Pots of l/5,000 a. are ahcared with paddy field soil and then filled with water. Paddy rice seedlings (Jukkoku variety) at the 3 to 4 leaves stage are transplanted into the pots under irrigated conditions. After the seedlings have taken root, seeds of barnyard grass and broad-leaved weeds are sown and spikerush are planted in such pots simultaneously.

The preparations of the given active compound are sprayed at the rate of 500, 250 and g of active compound per 10 a. onto the soil of pots. After 3 weeks, the degree of damage against the barnyard grass, spikerush and broad-leaved weeds and the phytotoxicity to the paddy rice are determined and characterized by the values 0 to 5, which have the following scales:

Herbicidal efficacy Phytotoxicity Table l Herbicidal effect against weeds of paddy fields and phytotoxicity to :rice

Active Amount Compound of active Herb icidal effect Phytotoxicity No. (see compound Table 5) in g/ 10 a. bamyardspikerush broadpaddy rice grass leaved weeds Compounds of Invention 500 5 5 5 l (1,) 250 S 4 4 O 125 5 3 3 0 500 5 5 5 2 (2,) 250 5 4 4 1 I25 5 3 4 0 500 5 5 5 l (3,) 250 5 v 4 3 0 125 5 3 2 0 500 5 4 4 0 (4,) 250 4 4 4 0 I25 4 3 2 O 500 4 4 3 O (5,) 250 3 3 3 0 l25 3 2 3 0 Herbicidal effect Phytbtoxicity spikerush broadpaddy rice grass leaved weeds Table l-continued Herbicidal effect against weeds of paddy fields and phylotoxicity to rice Active Amount Compound of active No. (see compound Table 5) in g/lO a. barnyard 000 00 00 00 00 00 0 0O OO OO OO -OO OO OOOOOOOO 0000 0050050050050050050 0500500500500500500500500500500500500500500500500500500500500500 0 20520520520520520 5-LO57-0520520 20520 20520520520520520520520520520520520520520520 Sa 52 52 52 52 52 5 2 52 52 52 52 52 52 52 52 52 5252 52 52 52 52 52 52 52 52 52 5a O O O 0 0 O J. O J. 1 1 l O l 2 3 4 5 .6 7 8 9 0 l, 2 3 4 5 Am 7 om 0n 0 .h L 3 V U W w l l l l l l I. l l 1 2 2 2 2 2 2 2 2 2 2 3 3 3 3 Table l-continued paddy fields and phytotoxicity to rice Active Amount Compound of active Herbicidal effect Phytotoxicity No. (see compound Table 5) in g/lO a. barnyardspikerush broadpaddy rice grass leaved weeds 125 45 2 3 O 500 5 5 5 (34,) 250 5 5 O 125 5 4 4 0 500 5 5 5 0 250 5 5 5 O 125 5 4 4-5 O 500 5 5 5 O (36 250 5 4-5 5 0 125 5 4 4 O 500 5 5 5 0 250 5 5 5 O 125 5 4 4 O 500 4 4 4 0 (38,) 250 3 3 3 0 125 3 2 3 O 500 5 4-5 5 0 250 5 4 5 O 1) 125 4 3 4-5 0 Known Compounds- Comparison (A) penta- 1000 5 5 5 5 chloro phenol (B) 2-methyl- 4chloro- 40 2 5 5 4 phenoxyacetic acid (C) S-Benzyl 500 4 3 5 O N,N-dimethyl 250 3 l 3 O -dithio- 125 2 O 2 0 carbamate (D) S-benzyl 500 5 5 5 4 N,N diiso- 250 4 4 4 3 propyl-thiol- 125 3 2-3 3 l carbamate Control 0 O O 0 NOTE:

Broad-leaved weeds are Nonochoria vaginalis, Rotala indica, Lindemia pyxidaria, Gratiola japonica, etc.

EXAMPLE 2 Test of pre-emergence soil treatment against various plants the degree of damage to the test plants is determined and characterized by the values 0 to 5, which have the following meaning:

To produce a suitable preparation of the particular active compound, 1 part by weight of such active compound is mixed with 5 parts by weight of solvent (acetone) and 1 part by weight of emulsifier (benzyloxypolyglycol ether), and the resulting emulsifiable concentrate is then diluted with water to the desired final concentration.

Seeds of the test plants are sown in normal soil and after 24 hours the preparation of the given active compound is sprayed onto the test plants After 3 weeks,

amount per unit area, and the results obtained can be seen from the following Table 2:

Table 2 Pre-emergence soil treatment against various plants (Pot test) Active Compound Amount No. (see of active Table 5) compound Cot- Cab- Echino- Portu- Cheno Stel- Amaran- Digiin kg/ha Wheat Barley Rice ton Maize bage chloa laca podium laria thus taria Compounds of Invention l 5 0 0 O 0 O 0 5 5 5 S 5 5 2.5 0 0 0 0 l 0 0 5 5 5 5 5 5 L25 0 0 O O O O 5 4 4 4 4 4 2O 5 5 5 5 5 5 5 5 5 5 5 5 [0 1-2 2 1-2 2 2 2 5 5 5 5 5 5 Table 2-continued Pre-emergence soil treatment against various plants (Pot test) Active Compound Amount No. (see of active Table 5) compound Cot- Cub- Echino- Portu- Cheno Stel- Amaran- Digiin kg/ha Wheat Barley Rice ton Maize bage chloa laca podium laria thus taria 1.25 O O 0 O O S 4 4 4 4 4 20 4 4 4 3 5 5 5 5 5 5 5 1-2 2 3 2 2 1-2 5 5 5 5 5 5 2) 5 0 0 0 O O 0 5 5 5 5 5 5 2.5 O 0 O O 0 0 5 5 5 5 5 5 1.25 O 0 O O 0 0 5 3-4 3-4 3-4 3-4 3-4 Known Compound- Comparison 20 3 3 3 4 3 5 5 5 5 5 5 5 (C) S-benzyl-N,N- 10 l-2 2 3 2 2 l-2 5 5 5 5 5 5 dimethyl-dithio- 5 O O O 0 O 0 4 5 5 5 5 5 carbamate 2.5 O O 0 0 O O 3 5 5 5 5 5 1.25 O 0 0 0 0 0 2 3 3 3 3 3 The following further examples are set forth to illus- EXAMPLE 3 trate, without limitation, the manner of producing the Test against spider mites (Pot test) Test method Approximately 50 adult spider mites are put on each corresponding cotyledon leaf of kidney beans planted in unglazed pots of 6 cm diameter. Tangle-foot is pasted on the petioles to prevent the mites from running away. The pots are kept in a greenhouse and two days later appropriate diluted solutions containing the desired concentration of the given active compound are sprayed on the leaves using a spray-gun. Ten days after the active compound spraying treatment, the number of surviving and killed adults and nymphs are counted.

The particular active compounds tested, their concentrations, and the results obtained can be seen from the following Table 2:

Table 3 Test against spider mites Concentration of Controlling effect active compound Active Compound No. (see Table 5) Compounds of Invention i+ii+++++i Known Compou nds- Comparison 0,0-diethyl- S-( 2,5-dichloro phenylmercaptomethyl)-phosph orodithiolate p-chloro-phenylp-chloro-benzene sulfonate Control instant compounds according to the present invention:

EXAMPLE 5 [VARIANT (A)] ocl-r ci-l 10.8 g (0.1 mol) of N,N-dimethyl-carbamoylchloride were dissolved in 200 ml of methylethyl ketone and 17.6 g (0.1 mol) of the sodium salt of o-methoxy-benzylmercaptan were added. The mixture was refluxed at 50-60C for about 5 hours with vigorous stirring. After the completion of the reaction, the reacted mixture was filtered, to separate off sodium chloride by-product, and crude crystals of o-methoxy-benzy1-N,N-dimethylthiolcarbamate were obtained with distilling off of methylethyl ketone from the filtrate. Yield: 19.4 g. M.p. 27-28.5C (recrystallized from alcohol).

In an analogous manner, upon reacting the appropriate sodium salt of p-methoxy-benzylmercaptan, 3- methyl-4-methoxy-benzylmercaptan and 2-methoxy-5- chloro-benzylmercaptan, respectively, with N,N- dimethyl-carbamoyl-chloride, the corresponding pmethoxy-benzyl-N,N-dimethyl-thiolcarbamate (1 of m.p. 2627C, 3-methyl-4methoxy-benzyl-N,N-dimethylthiolcarbamate (10 of bp l45-146C/0.1 mm Hg, and 2-methoxy-5-chloro-benzyl-N,N-dimethyl-thi olcarbamate (16 of m.p. 112.5ll3.5C, are ob- 25.1 g (0.1 mol) of 2-methoxy-S-chloro-benzyl-thiolcarbonyl-chloride were dissolved in 200 ml of ether and 14.6 g (0.2 mol) of diethylamine were added dropwise. The mixture was refluxed gently at 2025C for about 3 hours. After completing the reaction, separating by filtration the amine salt which had precipitated,

and distilling off ether from the filtrate, Z-methoxy-S- chloro-benzyl-N,N-diethyl-thiolcarbamate was obtained. Yield: 24.4 g B. p. l60l6lC/O.1 mm Hg.

In an analogous manner, upon reacting methyl-nbutyl-amine, di-n-propyl-amine and diisopropylamine, respectively, with Z-methoxy-S-chloro-benzyl-thiolcarbonylchloride, the corresponding Z-methoxy-S-chlorobenzyl-N,N-dialkyl-thiolcarbamates are obtained, i.e.,

Table 5-continued i Compound Structural formula,

Physical property (m.p. or b.p.)

OCH

OCH;

. l60-163 C/0.05 mm Hg 149 150c/0.5 mm Hg Table 5-c0ntinued Compound Stru ctural formula Physical property Table -continued Physical property The foregoing compounds may be designated:

1. 4-methoxy-benzyl-N,N-dimethyl-thiolcarbamate 2. 4-methoxy-benzyl-N,N-diethyl-thiolcarbamate 3. 4-methoxy-benzyl-N,N-diisopropyl-thiolcarbamate 4. 4-methoxy-benzyl-N-methyl-N-n-butyl-thiolcarbamate 5. 4-methoxy-benzyl-pyrrolidino-carbothiolic ester 6. 4-methoxy-benzyl-piperidino-carbothiolic acid ester 7. 3-methoxy-benzyl-N,N-dimethyl-thiolcarbamate 8. 2-methoxy-benzyl-N,N-dimethyl-thiolcarbamate 9. 2-methoxy-benzyl-N,N-diethyl-thiolcarbamate 10. 3-methyl-4-rnethoxy-benzyl-N,N-dimethyl-thiolcarbamate 1 1. 3-methyl-4-methoxy-benzyl-N,N-diethyl-thiolcarbamate 12. 2-methoxy-5-methyl-benzyl-N,N-dimethyl-thiolcarbamate 13. 2-methoxy-5-methyl-benzyl-N,N-diethyl-thiolcarbamate l4. 3-chloro-4-methoxy-benzyl-N,N-dimethyl-thiolcarbamate 15. 3-chlo ro-4-methoxybenzyl-N,N-diethyl-thiolcarbamate 16. Z-methoxy-S-chlor0-benzyl-N,N-dimethyl-thiolcarbamate l7. 2-methoxy-5-chloro-benzyl N,N-diethyl-thiolcarbamate 18. 2-methoxy-5-chloro-benzyl-N,N-diisopropyl-thiolcarbamate 19. 2-methoxy-5-chloro-benzyl-N,N-di-n-propyl-thiolcarbamate 20. 2-methoxy-5-chloro-benzyl-N-methyl-N-n-butylthiolcarbamate 21 4-ethoxy-benzyl-N,N-dimethyl-thiolcarbamate 22. 4-ethoxy-benzyl-N,N-diethyl-thiolcarbamate 23. 4-isopropoxy-benzyl-N,N-dimethyl-thiolcarbamate 24. 4-isopropoxy-benzyl-N,N-diethyl-thiolcarbamate 25. 3-chloro-4-ethoxy-benzyl-N,N-dimethyl-thiolcarbamate 26. 3-chloro-4-ethoxy-benzyl-N,N-diethyl-thiolcarbamate 27. 2-ethoxy-5-chloro-benzyl-N,N-dimethyl-thiolcarbamate 28. 2-ethoxy-5-chloro-benzyl-N,N-diethyl-thiolcarbamate 29. 3-nitro-4-methoxy-benzyl-N,N-dimethyl-thiolcarbamate acid 30. 4-methoxy-benzyl-N-methyl-thiolcarbamate 3 1 2-methoxy-5-brom0-benzyl-N,N-dimethyl-thiolcarbamate 3 2. 2-methoxy-5-tert. -butyl-benzyl-N ,N-dimethyl-thiolcarbamate 4-methoxy-5-br0mo-benzyl-N,N-diethyl-thiolcarbamate 34. 4-isopropyl-5-methyl-benzyl-N,N-dimethyl-thiolcarbamate 35. 4-isopropyl-5-methyl-benzyl-N,N-diethyl-thiolcarbamate r 36. 4-isopropyl-5-chloro-benzyl-N,N-dimethyl-thiolcarbamate 37. 2-isopropyl-5-chloro-benzyl-N,N-ethyl-thiolcarbamate 38. 2-methoxy-5-methyl-benzyl-N-methyl-thiolcarbamate 39. 4-ethoxy-5-methyl-benzyl-N,N-diethyl-thiolcarbamate It will be realized by the artisan that all of the foregoing compounds contemplated by the present invention possess the desired selective or total herbicidal properties, and especially the capability of selectively destroying weeds, and additionally acaricidal and nematocidal properties, as well as a comparatively low toxicity toward warm-blooded creatures and a concomitantly low phytotoxicity with respect to higher plants, enabling such compounds to be used with correspondingly favorable compatibility with respect to warmblooded creates and higher plants for more effective control and/or elimination of weeds, mites and nematodes by selective application of such compounds to such weeds, mites, nematodes and/or their habitat. Nevertheless, the instant compounds possess total herbicidal action when used in large quantities, although selective herbicidal action is obtained when used in smaller quantities. As contemplated herein, the term weeds is meant to include not only weeds in the narrow sense, but also in the broad sense, whereby to cover all plants and vegetation considered undesirably for the particular purposes in question.

It will be appreciated that the instant specification and examples are set forth by way of illustration and not limitation, and that various modifications and changes may be made without departing from the spirit and scope of the present invention.

What is claimed is:

1. A substituted benzyl-thiolcarbamic acid ester of the formula of chloro, bromo and C alkyl. 

1. A SUBSTITUTED BENZYL-THIOLCARBANIC ACID ESTER OF THE FORMULA
 2. A compound according to claim 1 wherein X is selected from the group consisting of chloro, bromo and C1-3 alkyl.
 3. A compound according to claim 1 wherein R is C1-3 alkyl, and X is selected from the group consisting of chloro, bromo and C1-2 alkyl. 